SAS Technical- Regulatory and Management Specialist

Job Description Roles & Responsibilities Data Management & Analytics Lead the end-to-end process of risk data management including capturing, organizing, storing, and analyzing. Perform data analytics to support regulatory and management reporting. Troubleshoot data-related issues and authorize necessary maintenance or modifications. Assist in data extraction (system and manual) and preparation for required reports. Consolidate data from multiple sources and deliver it in the agreed format using SAS and SQL expertise. Execute BAU (Business-As-Usual) activities across applications and systems. Addressing the data requirements from CBUAE along with looking at the automation aspects of the same as a part of TO-BE process. Implementation & Change Collaborate with IT teams to test and validate data accuracy and migration. Review current data logics and SAS coding for retail and regulatory reports. Update and enhance the coding based in line with regulatory guidelines and retail reporting mechanisms. Deploy automated reports using SAS Data Integration. Review current SOPs and enhance the documentation. Technology & Tools Apply statistical software (SAS, SQL) for analysis and support. Review and optimize existing SAS implementation code to improve processing efficiency. Integrate SAS Stratum with SAS Viya. Portfolio Management and IT Projects Engage in portfolio management projects including implementation of new requirements and data standards. Perform testing to ensure correct data migration and reporting. Configure the latest CBUAE requirements into SAS. Prepare and maintain Data Quality (DQ) reports aligned with portfolio data requirements as part of a structured data delivery framework. Automate existing manual regulatory and management reporting processes. Preferred Tools & Technologies: Power BI, SAP BusinessObjects, Oracle SAS, Python, R Relational Database Management Systems Desired Candidate Profile Bachelor's or Master's degree in Statistics, Computer Science, Bioinformatics, or a related quantitative field. Minimum of 5-7 years of progressive experience in SAS programming within the pharmaceutical or biotechnology industry. Proven expertise in applying SAS (Base SAS, SAS/STAT, SAS Macro) to clinical trial data analysis and regulatory reporting. Deep understanding of regulatory submission requirements (e.g., CDISC SDTM/ADaM standards, ICH guidelines). Skills Data Management SAS SQL Employment Type Full-time Company Industry RecruitmentPlacement FirmExecutive Search Department / Functional Area DBADatawarehousing (IT Software) Keywords Pharmaceutical SAS SpecialistClinical SAS Analyst - SubmissionsCDISC StandardsSAS Regulatory Data Solutions ArchitectData ManagementSAS ProgrammingSDTMRegulatory SAS Technical Expert Get real-time job updates only on our App